Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8298384 | Biochemistry and Biophysics Reports | 2018 | 9 Pages |
Abstract
Collectively, these data suggest that Nox1-mediated ROS production is required for UVB-induced cytotoxicity and inflammation through p38 activation and inflammatory cytokine production, such as IL-6. Thus, our findings suggest Nox1 as a therapeutic target for cytotoxicity and inflammation in response to UVB exposure.
Keywords
STAT3Jun N-terminal kinasesMKPO2-ASK1GM-CSFERKNACUVBJnkIL-6DPINF-κBPBSDNAH2DCFDAMAPKMAPK phosphataseMKKNADPH oxidase 1NOxROSHydrogen peroxidedeoxyribonucleic acidRNAribonucleic acidUltravioletNADPH oxidaseinterleukin-6Baxtumor necrosis factor-alphaDiphenyleneiodoniumHydroxyl radicalCytotoxicitySuperoxidegranulocyte-macrophage colony-stimulating factorTNF-αnuclear factor kappa Blactate dehydrogenaseLDHsignal transducer and activator of transcription 3Phosphate-buffered salineN-acetyl cysteineH2O2BCL2-associated X proteinmitogen-activated protein kinaseKeratinocyteMAP kinaseextracellular signal-regulated kinaseapoptosis signal-regulating kinase 1Reactive oxygen species
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Authors
Azela Glady, Manami Tanaka, Catharina Sagita Moniaga, Masato Yasui, Mariko Hara-Chikuma,